Multiple Sclerosis
Conditions
Brief summary
To evaluate the usability of positron emission tomography imaging as a novel outcome measure in multiple sclerosis studies
Detailed description
Background and Rationale In multiple sclerosis (MS), significant pathology correlating to disease progression, to expanded disability status scale (EDSS) and to cognitive decline, takes place outside the plaque areas, i.e. in areas of normal appearing white matter and gray matter. Neuropathological studies suggest that mechanisms involved in this widespread pathology include activation of microglial cells, oxidative stress and deficiency in mitochondrial functions. Activated microglia can be detected in vivo with a translocator protein (TSPO), expressed in activated, but not resting microglia) binding radioligands and positron emission tomography (PET). 11Carbon-PK11195 radioligand is one such radioligand. Importantly, the possible effect of MS therapies on microglial activity can be evaluated in patients in vivo with PET-imaging performed before and after the treatment.
Interventions
RADIATIONPET and MRI
Patients will be imaged using PET and MRI at baseline, and twice during treatment
Sponsors
Turku University Hospital
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to 58 Years
Healthy volunteers
No
Inclusion criteria
Having signed the informed consent of the investigator-initiated PET study * Age 18 - 58 years at the time of informed consent. * MS according to Poser or McDonald criteria * EDSS score from 0.0 to 6.5. * Moderate to heavy lesion load ( \>9 T2 lesions) in MRI
Exclusion criteria
* \- Patients with other neurodegenerative disease than MS * Disease modifying therapy (DMT) within 4 weeks of imaging * Corticosteroid treatment within 4 weeks of imaging * Patients with significant abnormal findings other than MS in the screening MRI. * Patients with claustrophobia, or a history of moderate to severe anxiety disorder or panic attacks (which could potentially lead to preterm termination of the imaging) * Contraindication to PET scan investigations * Exposure to experimental radiation in the past 12 months such that radiodosimetry limits would be exceeded by participating in this study. * Intolerance to previous PET scans; i.e. previous hypersensitivity reactions to any PET ligand or imaging agent or failure to participate in and comply with previous PET scans.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change of 11C-PK11195-radioligand binding using PET | 0 to 24 weeks | Patients will be switched to fingolimod from first-line therapies as per indication and as part of their normal treatment regimen, and those who will consent to participate in this investigator-initiated PET study, will be imaged at baseline (pre-treatment phase) and after 6-8 weeks and 24 weeks of treatment. Purpose is to compare the binding of the radioligand between these three time points. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| MRI metrics | 0, 6-8 wk, 24 wk | To evaluate the total lesion load of the white matter MS plaques with MRI; baseline vs. 6-8 weeks vs. 24 weeks of Gilenya treatment |
Countries
Finland
Outcome results
None listed